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本文引用的文献

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Advanced material strategies for tissue engineering scaffolds.高级材料策略在组织工程支架中的应用。
Adv Mater. 2009 Sep 4;21(32-33):3410-8. doi: 10.1002/adma.200900303.
2
Finite element analysis of an accordion-like honeycomb scaffold for cardiac tissue engineering.用于心脏组织工程的手风琴状蜂窝支架的有限元分析。
J Biomech. 2010 Nov 16;43(15):3035-43. doi: 10.1016/j.jbiomech.2010.06.032. Epub 2010 Jul 31.
3
Perfusion seeding of channeled elastomeric scaffolds with myocytes and endothelial cells for cardiac tissue engineering.心肌细胞和内皮细胞灌注接种管状弹性支架用于心脏组织工程。
Biotechnol Prog. 2010 Mar-Apr;26(2):565-72. doi: 10.1002/btpr.337.
4
Porous polycaprolactone scaffold for cardiac tissue engineering fabricated by selective laser sintering.采用选择性激光烧结技术制备用于心脏组织工程的多孔聚己内酯支架。
Acta Biomater. 2010 Jun;6(6):2028-34. doi: 10.1016/j.actbio.2009.12.033. Epub 2009 Dec 22.
5
Surface topography induces 3D self-orientation of cells and extracellular matrix resulting in improved tissue function.表面形貌诱导细胞和细胞外基质的 3D 自取向,从而改善组织功能。
Integr Biol (Camb). 2009 Feb;1(2):196-204. doi: 10.1039/b820208g. Epub 2009 Jan 15.
6
Electrospun fibrous scaffolds with multiscale and photopatterned porosity.具有多尺度和光图案化多孔性的静电纺丝纤维支架。
Macromol Biosci. 2010 Mar 10;10(3):265-70. doi: 10.1002/mabi.200900363.
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The influence of left-ventricular shape on end-diastolic fiber stress and strain.左心室形状对舒张末期纤维应力和应变的影响。
Annu Int Conf IEEE Eng Med Biol Soc. 2009;2009:2887-90. doi: 10.1109/IEMBS.2009.5333112.
8
A method to replicate the microstructure of heart tissue in vitro using DTMRI-based cell micropatterning.使用基于 DTMRI 的细胞微图案化技术在体外复制心脏组织微观结构的方法。
Ann Biomed Eng. 2009 Dec;37(12):2510-21. doi: 10.1007/s10439-009-9815-x. Epub 2009 Oct 6.
9
Engineering substrate topography at the micro- and nanoscale to control cell function.在微米和纳米尺度上设计基底形貌以控制细胞功能。
Angew Chem Int Ed Engl. 2009;48(30):5406-15. doi: 10.1002/anie.200805179.
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Microcontact printing and lithographic patterning of electrospun nanofibers.静电纺纳米纤维的微接触印刷和光刻图案化
Langmuir. 2009 Jun 2;25(11):6015-8. doi: 10.1021/la900811k.

联合技术用于微制造弹性心脏组织工程支架。

Combined technologies for microfabricating elastomeric cardiac tissue engineering scaffolds.

机构信息

Harvard-MIT Division of Health Sciences and Technology, Massachusetts Institute of Technology, Cambridge, Massachusetts, USA.

出版信息

Macromol Biosci. 2010 Nov 10;10(11):1330-7. doi: 10.1002/mabi.201000165.

DOI:10.1002/mabi.201000165
PMID:20718054
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3315382/
Abstract

Polymer scaffolds that direct elongation and orientation of cultured cells can enable tissue engineered muscle to act as a mechanically functional unit. We combined micromolding and microablation technologies to create muscle tissue engineering scaffolds from the biodegradable elastomer poly(glycerol sebacate). These scaffolds exhibited well defined surface patterns and pores and robust elastomeric tensile mechanical properties. Cultured C2C12 muscle cells penetrated the pores to form spatially controlled engineered tissues. Scanning electron and confocal microscopy revealed muscle cell orientation in a preferential direction, parallel to micromolded gratings and long axes of microablated anisotropic pores, with significant individual and interactive effects of gratings and pore design.

摘要

聚合物支架可以引导培养细胞的伸长和取向,从而使组织工程肌肉能够作为机械功能单元发挥作用。我们结合微成型和微刻蚀技术,从可生物降解弹性体聚(癸二酸甘油酯)中制造出肌肉组织工程支架。这些支架具有明确定义的表面图案和孔以及坚固的弹性拉伸力学性能。培养的 C2C12 肌肉细胞渗透到孔中,形成空间可控的工程组织。扫描电子显微镜和共聚焦显微镜显示,肌肉细胞沿优选方向取向,与微成型光栅和微刻蚀各向异性孔的长轴平行,光栅和孔设计具有显著的个体和交互作用。